It has been a hectic week and I have felt like crap
throughout. Currently I am enjoying a Renaissance Cherry Porter, so bliss is
very near. This gives me an opportunity to recap on my week and hopefully
restrain me from complaining too much.
Here we go…
I feel I may have built up far too much suspense in
the ending of the previous paragraph. Sorry about that. Essentially, last week I had chemo Monday,
overdid things Friday and spent Saturday and Sunday paying for it dearly. Sunday, I busied myself in differing positions of horizontal; lying in bed, lying on the
couch, lying on the floor. I was so exhausted I could not even formulate
replies to text messages. Sorry to those affected by this. I know hearing from
me is the highlight of everybody’s lives. Fortunately, sleep came readily; I
did not even need my nearly-empty-calorie-pills, which is good because I did
not have any left, and my biological resistance to slumber inducing substances
has reached the level where one antihistamine just doesn’t cut the mustard.
I suspect this current bout of woefulness is in part due to
dread. My second cycle of chemo is now complete and this is a magic line in the
sand kind of moment, as my treatment and prognosis after this point is
dependent on the progress of the chemo thus far. I am sure that all makes sense. Basically, I
had a PET scan prior to my first chemo, and another one yesterday. If the
tumours have reduced in size and prevalence, then yay, I stay with ABVD. If
not, then treatment options need to be reassessed. This could mean a relatively
new regime named escalated BEACOPP (I know very little about it) or, although
highly unlikely, an autologous stem cell transplant. I will explain what that
means if or when I need to. I won’t find out what my next type of treatment
will be until Monday, when the results of my scan are known. Fun times.
Shall we talk about the PET scan then? I had intended this as
separate entry, another retrospective one, however I never got around to it so
I will do it now. The science behind this is quite cool. They inject a radioactive
variant of glucose into you whilst you are in a fasted state. Tumour cells
metabolise glucose at a much higher rate than regular cells, so in the PETCT
scan they show up all red and angry, while the normal cells are grey and
boring. We like boring. Everyone hope for boring. Right, so, I have to be in a fasting
state, on the first scan this was fine, it was a 10am scan so it was no big
deal. Yesterday it was a 1pm scan; I went from fasting to famished. I had
retired to bed at a spritely 9pm the night prior, so by the time my appointment
rocked around I’d passed hangger and moved on to total lethargy. I gave vague
responses to the multitude of poorly put questions. They were particularly
unimpressed with my response to the “Any chance you could be pregnant?” question;
“I am pretty sure the chemo would put stop to anything like that”. Not the correct
answer, just an FYI. It is crazy that pre-treatment they prep you on the odds
of infertility and the like, and then any chance they get they like to ask you
if you’re pregnant. I am not, I do not plan to be, and I am pretty sure my body
wouldn’t be able to handle it if I was. It would tag out. Game over. Ok so no
jokes allowed, granted it was a rather dark one, but I guess we are technically
dealing with physicists here.
Once that rather dicey question has been inadequately
answered we get down to the fun stuff. The lady (whom I fear I have portrayed
negatively when actually she was quite lovely) fetches her radioactive glucose,
it is kept in a metal case, in a metal syringe, and looks like something out of
a Bond movie; she is donning a full lab coat, gloves and a radiation counter.
The cannula is inserted into my right arm (last week’s chemo arm, so already in
an utterly pitiful state), and promptly the substance is flushed through my veins.
Boom! I am radioactive. I feel like I should have gone all Peter Parker on
everyone. Unfortunately I was instructed to lie as still as possible for an
hour. Absolutely no leaping with spider like projections from buildings. Damn. I am not even able to read, as that demands an unfair proportion of glucose for my brain and they would like the
distribution to be equal throughout my body, please. As I have mentioned, I was
feeling crap, very very very crap. I think I may have slept; the drool present
on my face when I was collected would definitely lead to such a conclusion. I
was instructed to ‘pee’ (he actually used the word pee, which at least drew a
smile out of me) using a separate toilet, as I am radioactive you know.
Then comes the scan. The scan sucks. You have to lay totally
still for like 30 minutes, whilst going in and out of a prolonged CT scanner.
Oh and you have to keep your hands above your head, still. This was hard enough
pre dacarbazine - have I mentioned how much dacarbazine makes my arm ache? –
but post chemo it was horrendous. Deep breathing and, I believe, some quick
scanning by a fellow antipodean, meant I got through it with only the bare
minimum of tears. I think at one point I may have shouted “I can’t go on!” a
total “Do it to Julia” moment. Big brother was totally watching, cameras,
microphones, the works. Who would have thought room 101 for me was purely
keeping my hands above my head for half an hour? And I was a basketballer. I
need to toughen up.
That brings me to today. I cannot recall if I have yet mentioned that my arm hurts a mighty lot after chemo. Well it does. It does so
much that I have neglected to write this entry into my little black book, as my
right arm was my chemo arm this time, and it is unable to hold a pen. So I am
going full tilt on the typing, which to be honest, does little to relieve the
pain. But do not fear dear readers! I have come across a solution. This
solution is a PICC line, which I had inserted today. A PICC line is inserted
just above the elbow joint. Using ultra sound and local anaesthetic, a wire is
thread through the vein, running just under the fourth rib and into the heart.
A tube then surrounds the wire, and a cannula is attached to the tube. No more
needles, and a lovely little protective sheath for the dacarbazine (if indeed
that is the drug of choice) to pass through rather than the vein. And, above
all, hopefully no more bloody arm pain. Except now I don’t know which pain is
caused by the darcabazine, and which pain is caused by the PICC line. What I
can tell you is that occasionally I feel the line tickling my heart, which is a
little disconcerting. It does cause sporadic heart palpitations, but it doesn’t
hurt anywhere near as much as my spleen. I don’t think a splenectomy is on the
cards, so don’t get your hopes up on avoiding that complaint. And the rest of
my arm is still in agony from last week’s darcabazine, so I will be inclined to
moan about that for a wee while longer.
Does this thing work for caffeine or alcohol as well? |
That is my week thus far, I keep thinking paracetamol doesn’t
touch the darcabazine arm pain, but then the drug wears off and anguish again
sets in. I have a proper purple vein this time, still a little bruising, and a
slight uncomfortable feeling in my chest when I slouch or breathe too deeply.
They have x-rayed my chest to see where the line is sitting and everything is
as it should be, so I guess it will be a feeling that, in time, I will become
accustomed to.
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